Incidental Mutation 'IGL01665:Cyp3a11'
ID 103291
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp3a11
Ensembl Gene ENSMUSG00000056035
Gene Name cytochrome P450, family 3, subfamily a, polypeptide 11
Synonyms Cyp3a, Pcn, IIIAm1
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01665
Quality Score
Status
Chromosome 5
Chromosomal Location 145791417-145816664 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 145805475 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 181 (M181L)
Ref Sequence ENSEMBL: ENSMUSP00000037665 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035918]
AlphaFold Q64459
Predicted Effect probably benign
Transcript: ENSMUST00000035918
AA Change: M181L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000037665
Gene: ENSMUSG00000056035
AA Change: M181L

DomainStartEndE-ValueType
Pfam:p450 38 494 2.4e-136 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsbg1 T A 9: 54,530,004 (GRCm39) I231L probably benign Het
Adcyap1 T A 17: 93,507,506 (GRCm39) V22D probably damaging Het
Adgra3 T C 5: 50,164,272 (GRCm39) T236A possibly damaging Het
Adipor2 A T 6: 119,338,887 (GRCm39) L122H probably benign Het
Atp1a4 T C 1: 172,074,291 (GRCm39) I321V probably benign Het
Bhmt2 A T 13: 93,799,661 (GRCm39) Y258* probably null Het
C230029F24Rik T A 1: 49,377,253 (GRCm39) noncoding transcript Het
Ccpg1 T A 9: 72,913,159 (GRCm39) F232I probably damaging Het
Cd83 A T 13: 43,955,153 (GRCm39) T195S probably benign Het
Cdcp3 G T 7: 130,848,386 (GRCm39) G847* probably null Het
Cfap70 G A 14: 20,453,186 (GRCm39) T897M probably damaging Het
Frem2 C T 3: 53,457,083 (GRCm39) V2090I probably benign Het
Gm45234 A G 6: 124,723,571 (GRCm39) probably benign Het
Gm7964 T A 7: 83,406,341 (GRCm39) noncoding transcript Het
Igsf9 T A 1: 172,319,738 (GRCm39) C39* probably null Het
Il1rap A T 16: 26,541,463 (GRCm39) D568V probably damaging Het
Ints7 C T 1: 191,345,331 (GRCm39) probably benign Het
Lsamp C T 16: 41,964,375 (GRCm39) R250* probably null Het
Oit3 T A 10: 59,274,731 (GRCm39) D23V probably damaging Het
Pcdh17 T A 14: 84,684,442 (GRCm39) L303Q probably damaging Het
Pcdhb1 T A 18: 37,400,450 (GRCm39) N800K probably benign Het
Plce1 A G 19: 38,513,331 (GRCm39) D210G probably benign Het
Plekhb2 T A 1: 34,908,411 (GRCm39) Y152N probably damaging Het
Rbp3 T C 14: 33,678,088 (GRCm39) S679P probably benign Het
Rps6kc1 T C 1: 190,643,854 (GRCm39) T2A possibly damaging Het
Tmem167 T A 13: 90,246,504 (GRCm39) S9R probably damaging Het
Xpnpep1 A T 19: 52,985,463 (GRCm39) S522T probably benign Het
Other mutations in Cyp3a11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00848:Cyp3a11 APN 5 145,799,275 (GRCm39) missense probably damaging 1.00
IGL01316:Cyp3a11 APN 5 145,791,961 (GRCm39) missense possibly damaging 0.78
IGL01348:Cyp3a11 APN 5 145,805,817 (GRCm39) missense possibly damaging 0.80
IGL01591:Cyp3a11 APN 5 145,812,291 (GRCm39) splice site probably benign
IGL02203:Cyp3a11 APN 5 145,805,976 (GRCm39) missense probably damaging 1.00
IGL02894:Cyp3a11 APN 5 145,805,836 (GRCm39) nonsense probably null
IGL03201:Cyp3a11 APN 5 145,797,189 (GRCm39) missense possibly damaging 0.94
IGL03342:Cyp3a11 APN 5 145,791,927 (GRCm39) missense probably damaging 0.96
PIT4486001:Cyp3a11 UTSW 5 145,797,302 (GRCm39) missense probably damaging 0.99
R0347:Cyp3a11 UTSW 5 145,802,735 (GRCm39) missense possibly damaging 0.93
R0376:Cyp3a11 UTSW 5 145,799,262 (GRCm39) nonsense probably null
R0378:Cyp3a11 UTSW 5 145,805,417 (GRCm39) missense probably benign 0.43
R0448:Cyp3a11 UTSW 5 145,799,204 (GRCm39) missense probably benign 0.00
R0567:Cyp3a11 UTSW 5 145,805,959 (GRCm39) missense probably damaging 1.00
R0968:Cyp3a11 UTSW 5 145,799,324 (GRCm39) splice site probably benign
R1292:Cyp3a11 UTSW 5 145,802,804 (GRCm39) missense probably benign 0.04
R1400:Cyp3a11 UTSW 5 145,799,299 (GRCm39) missense probably damaging 0.98
R1478:Cyp3a11 UTSW 5 145,795,581 (GRCm39) missense probably benign 0.01
R1520:Cyp3a11 UTSW 5 145,799,263 (GRCm39) missense probably damaging 1.00
R1716:Cyp3a11 UTSW 5 145,805,776 (GRCm39) missense probably benign
R2060:Cyp3a11 UTSW 5 145,791,891 (GRCm39) missense probably benign 0.00
R2076:Cyp3a11 UTSW 5 145,816,576 (GRCm39) missense probably benign
R2227:Cyp3a11 UTSW 5 145,805,357 (GRCm39) missense possibly damaging 0.90
R3725:Cyp3a11 UTSW 5 145,802,810 (GRCm39) missense probably benign 0.02
R4222:Cyp3a11 UTSW 5 145,797,276 (GRCm39) missense probably damaging 0.99
R4256:Cyp3a11 UTSW 5 145,806,005 (GRCm39) missense probably benign 0.04
R4294:Cyp3a11 UTSW 5 145,806,005 (GRCm39) missense probably benign 0.04
R4852:Cyp3a11 UTSW 5 145,797,305 (GRCm39) missense probably damaging 1.00
R5229:Cyp3a11 UTSW 5 145,791,945 (GRCm39) missense probably benign 0.00
R5285:Cyp3a11 UTSW 5 145,791,893 (GRCm39) missense probably benign 0.00
R5590:Cyp3a11 UTSW 5 145,802,787 (GRCm39) missense probably benign 0.00
R5703:Cyp3a11 UTSW 5 145,797,183 (GRCm39) missense probably benign
R5786:Cyp3a11 UTSW 5 145,799,284 (GRCm39) missense possibly damaging 0.47
R6291:Cyp3a11 UTSW 5 145,799,237 (GRCm39) missense possibly damaging 0.89
R6405:Cyp3a11 UTSW 5 145,799,230 (GRCm39) missense probably damaging 0.96
R6892:Cyp3a11 UTSW 5 145,797,258 (GRCm39) missense probably damaging 0.98
R7114:Cyp3a11 UTSW 5 145,795,593 (GRCm39) missense probably benign 0.16
R7243:Cyp3a11 UTSW 5 145,795,613 (GRCm39) missense probably damaging 0.96
R7438:Cyp3a11 UTSW 5 145,802,710 (GRCm39) missense probably benign 0.39
R7611:Cyp3a11 UTSW 5 145,797,191 (GRCm39) missense probably benign 0.25
R8346:Cyp3a11 UTSW 5 145,795,612 (GRCm39) missense probably damaging 1.00
R8371:Cyp3a11 UTSW 5 145,805,438 (GRCm39) missense possibly damaging 0.92
R8895:Cyp3a11 UTSW 5 145,797,330 (GRCm39) missense probably benign
R9043:Cyp3a11 UTSW 5 145,805,995 (GRCm39) missense probably benign 0.02
R9300:Cyp3a11 UTSW 5 145,799,164 (GRCm39) missense possibly damaging 0.60
R9404:Cyp3a11 UTSW 5 145,799,258 (GRCm39) missense probably benign 0.40
Posted On 2014-01-21